Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
Overview
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology is a scientific journal, published since 1997 in English. The journal's country of origin is Italy.
Details
Details
Abbr.
Acta Myol
Start
1997
End
Continuing
Frequency
Three no. a year
p-ISSN
1128-2460
e-ISSN
2532-1900
Country
Italy
Language
English
Metrics
Metrics
h-index / Ranks: 8879
39
SJR / Ranks: 7701
585
CiteScore / Ranks: 8773
2.90
Recent Articles
1.
Annunziata A, Langella G, Cauteruccio R, Fiorentino L, Fiorentino G
Acta Myol
. 2025 Feb;
43(4):149-152.
PMID: 40017292
Bethlem myopathy (BM) was first described in 1976 by Bethlem and van Wijngaarden in patients who presented a myopathy characterized by slowly progressive muscle weakness and typical flexion contractures of...
2.
Porcino M, Guccione F, Usbergo C, Navarra G, Toscano A, Musumeci O
Acta Myol
. 2025 Feb;
43(4):145-148.
PMID: 40017291
Objective: This case study aimed to evaluate the safety and efficacy of sleeve gastrectomy surgery in an obese patient with Late-onset Pompe disease (LOPD) and to explore the potential role...
3.
Caputo M, Schoser B
Acta Myol
. 2025 Feb;
43(4):139-144.
PMID: 40017290
Objectives: Pathogenic TRIM32 gene variant was first described in 1976 in the Hutterite population of North America, presenting a phenotype of Limb-girdle muscular dystrophy R8 (LGMDR8, formerly termed LGMD2H). In...
4.
Lucchiari S, Magri F, Rimoldi M, Pagliarani S, Corti S, Comi G, et al.
Acta Myol
. 2025 Feb;
43(4):134-138.
PMID: 40017289
Objective: Myotonic dystrophy type 2 (DM2; PROMM) is characterized by myotonia and muscle dysfunction, episodic muscle pain, proximal and axial weakness of the neck flexors. We describe the case of...
5.
Baille G, Severa G, Verebi C, Carlier R, Malfatti E
Acta Myol
. 2025 Feb;
43(4):130-133.
PMID: 40017288
Tubular aggregate myopathy is a rare neuromuscular condition associated with the presence of myofibers protein accumulations, in the form of dense tubular aggregates. Clinically it is characterized by proximal muscular...
6.
Caputo M, Schoser B
Acta Myol
. 2025 Feb;
43(4):123-129.
PMID: 40017287
Objectives: Mutations in the FHL1 gene have been associated with a diverse spectrum of X-linked diseases affecting skeletal and cardiac muscle. Six clinically distinct human myopathies can be recognized, including...
7.
Gadaleta G, Urbano G, Rolle E, Topf A, Vercelli L
Acta Myol
. 2024 Oct;
43(3):116-118.
PMID: 39468969
Introduction And Aims: We describe a case of long-living COLQ-related congenital myasthenic syndrome (CMS) benefitting from ephedrine with an overall improvement quantified with functional measures. Results: A 71-year-old man was...
8.
Bello L, Sansone V, Masson R, Bruno C
Acta Myol
. 2024 Oct;
43(3):114-115.
PMID: 39468968
No abstract available.
9.
Pugliese A, Migliorato A, Barbaccia A, Biasini F, Musumeci O, Toscano A, et al.
Acta Myol
. 2024 Oct;
43(3):108-113.
PMID: 39468967
Objectives: Focal myositis (FM) is a rare and restricted skeletal muscle inflammation, presenting as a solid mass with a typical lower leg localization and benign prognosis. In most cases the...
10.
Spagnoli C, Adorisio R, Bello L, DAmico A, DAngelo M, Pane M, et al.
Acta Myol
. 2024 Oct;
43(3):102-107.
PMID: 39468966
Objectives: Duchenne Muscular Dystrophy (DMD) is a severe, progressive, X-linked disorder resulting in muscle wasting, progressive functional loss and cardiomyopathy. Therapeutic strategies feature glucocorticoid corticosteroids plus gene therapy/stop codon read-through,...